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Prognostic survival model for people diagnosed with invasive cutaneous melanoma
BACKGROUND: The ability of medical practitioners to communicate risk estimates effectively to patients diagnosed with melanoma relies on accurate information about prognostic factors and their impact on survival. This study reports the development of one of the few melanoma prognostic models, called...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328047/ https://www.ncbi.nlm.nih.gov/pubmed/25637143 http://dx.doi.org/10.1186/s12885-015-1024-4 |
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author | Baade, Peter D Royston, Patrick Youl, Philipa H Weinstock, Martin A Geller, Alan Aitken, Joanne F |
author_facet | Baade, Peter D Royston, Patrick Youl, Philipa H Weinstock, Martin A Geller, Alan Aitken, Joanne F |
author_sort | Baade, Peter D |
collection | PubMed |
description | BACKGROUND: The ability of medical practitioners to communicate risk estimates effectively to patients diagnosed with melanoma relies on accurate information about prognostic factors and their impact on survival. This study reports the development of one of the few melanoma prognostic models, called the Melanoma Severity Index (MSI), based on population-based cancer registry data. METHODS: Data from the Queensland Cancer Registry for people (20–89 years) diagnosed with a single invasive melanoma between 1995 and 2008 (n = 28,654; 1,700 melanoma deaths). Additional clinical information about metastasis, ulceration and positive lymph nodes was manually extracted from pathology forms. Flexible parametric survival models were combined with multivariable fractional polynomial for selecting variables and transformations of continuous variables. Multiple imputation was used for missing covariate values. RESULTS: The MSI contained the variables thickness (transformed, explained 40.6% of variation in survival), body site (additional 1.9% in variation), metastasis (1.8%), positive nodes (0.7%), ulceration (1.3%), age (1.1%). Royston and Sauerbrei’s D statistic (measure of discrimination) was 1.50 (95% CI = 1.44, 1.56) and the corresponding RD2 (measure of explained variation) was 0.47 (0.45, 0.49), demonstrating strong explanatory performance. The Harrell-C statistic was 0.88 (0.88, 0.89). Lacking an external validation dataset, we applied internal-external cross validation to demonstrate the consistency of the prognostic information across geographically-defined subsets of the cohort. CONCLUSIONS: The MSI provides good ability to predict survival for melanoma patients. Beyond the immediate clinical use, the MSI may have important public health and research applications for evaluations of public health interventions aimed at reducing deaths from melanoma. |
format | Online Article Text |
id | pubmed-4328047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43280472015-02-15 Prognostic survival model for people diagnosed with invasive cutaneous melanoma Baade, Peter D Royston, Patrick Youl, Philipa H Weinstock, Martin A Geller, Alan Aitken, Joanne F BMC Cancer Research Article BACKGROUND: The ability of medical practitioners to communicate risk estimates effectively to patients diagnosed with melanoma relies on accurate information about prognostic factors and their impact on survival. This study reports the development of one of the few melanoma prognostic models, called the Melanoma Severity Index (MSI), based on population-based cancer registry data. METHODS: Data from the Queensland Cancer Registry for people (20–89 years) diagnosed with a single invasive melanoma between 1995 and 2008 (n = 28,654; 1,700 melanoma deaths). Additional clinical information about metastasis, ulceration and positive lymph nodes was manually extracted from pathology forms. Flexible parametric survival models were combined with multivariable fractional polynomial for selecting variables and transformations of continuous variables. Multiple imputation was used for missing covariate values. RESULTS: The MSI contained the variables thickness (transformed, explained 40.6% of variation in survival), body site (additional 1.9% in variation), metastasis (1.8%), positive nodes (0.7%), ulceration (1.3%), age (1.1%). Royston and Sauerbrei’s D statistic (measure of discrimination) was 1.50 (95% CI = 1.44, 1.56) and the corresponding RD2 (measure of explained variation) was 0.47 (0.45, 0.49), demonstrating strong explanatory performance. The Harrell-C statistic was 0.88 (0.88, 0.89). Lacking an external validation dataset, we applied internal-external cross validation to demonstrate the consistency of the prognostic information across geographically-defined subsets of the cohort. CONCLUSIONS: The MSI provides good ability to predict survival for melanoma patients. Beyond the immediate clinical use, the MSI may have important public health and research applications for evaluations of public health interventions aimed at reducing deaths from melanoma. BioMed Central 2015-01-31 /pmc/articles/PMC4328047/ /pubmed/25637143 http://dx.doi.org/10.1186/s12885-015-1024-4 Text en © Baade et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Baade, Peter D Royston, Patrick Youl, Philipa H Weinstock, Martin A Geller, Alan Aitken, Joanne F Prognostic survival model for people diagnosed with invasive cutaneous melanoma |
title | Prognostic survival model for people diagnosed with invasive cutaneous melanoma |
title_full | Prognostic survival model for people diagnosed with invasive cutaneous melanoma |
title_fullStr | Prognostic survival model for people diagnosed with invasive cutaneous melanoma |
title_full_unstemmed | Prognostic survival model for people diagnosed with invasive cutaneous melanoma |
title_short | Prognostic survival model for people diagnosed with invasive cutaneous melanoma |
title_sort | prognostic survival model for people diagnosed with invasive cutaneous melanoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4328047/ https://www.ncbi.nlm.nih.gov/pubmed/25637143 http://dx.doi.org/10.1186/s12885-015-1024-4 |
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